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HRID 405802生成日期:2026年10月26日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → Tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/405802

反应方程式

参与物

角色名称HCID投料
反应物聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
反应物Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
反应物1-(叔丁氧基羰基)氮杂环丁烷-3-乙酸HCID 11095989—
反应物N-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677441—
溶剂甲基吡咯烷酮HCID 13387—
产物Tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylateHCID 71281398—

反应条件

温度125 °C

反应步骤

Carbonyl diimidazole (CDI) (52.0 mg, 0.32 mmol) was added to a stirred solution of 2-(1-(tert-butoxycarbonyl)azetidin-3-yl)acetic acid (69.0 mg, 0.32 mmol) in NMP (1.0 mL). After 20 minutes, N-(5-(N′-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (9) (49.5 mg, 0.16 mmol) was added in one portion and the resulting solution was stirred for 30 minutes before it was heated at 125° C. for 15 minutes in a microwave reactor. The reaction mixture was added dropwise to water (20 mL) with stirring. The precipitate was filtered and dried to give tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylate (54). MS m/z 489.2 (M+1)+.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08754071B2
来源数据集uspto-grants-2014_06
ORD IDord-6cdf3e92c7e2492dab844346282e1328
来源说明uspto-grants-2014_06